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TATAGCCCATTCTTGTAACTTCTAT[C/G]TCTTCCCTACAACGTTTGGGATTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611831 | ||||||||||||||||||||
Literature Links: |
MRPL18 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
MRPL18 - mitochondrial ribosomal protein L18 | ||||||
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There are no transcripts associated with this gene. |
PNLDC1 - PARN like, ribonuclease domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271862.1 | 362 | Missense Mutation | CTC,GTC | L,V 93 | NP_001258791.1 | |
NM_173516.2 | 362 | Missense Mutation | CTC,GTC | L,V 82 | NP_775787.1 | |
XM_011535491.2 | 362 | Missense Mutation | CTC,GTC | L,V 82 | XP_011533793.1 | |
XM_011535493.2 | 362 | Intron | XP_011533795.1 | |||
XM_017010312.1 | 362 | Missense Mutation | CTC,GTC | L,V 125 | XP_016865801.1 | |
XM_017010313.1 | 362 | Missense Mutation | CTC,GTC | L,V 87 | XP_016865802.1 | |
XM_017010314.1 | 362 | Missense Mutation | CTC,GTC | L,V 125 | XP_016865803.1 | |
XM_017010315.1 | 362 | Missense Mutation | CTC,GTC | L,V 55 | XP_016865804.1 | |
XM_017010316.1 | 362 | Missense Mutation | CTC,GTC | L,V 44 | XP_016865805.1 |